Manganese pentacarbonyl bromide

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Manganese pentacarbonyl bromide
BrMn(CO)5.png
BrMn(CO)5.jpg
Names
Other names
bromopentacarbonylmanganese
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.035.005 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 238-522-8
PubChem CID
  • InChI=1S/5CO.BrH.Mn/c5*1-2;;/h;;;;;1H;/q;;;;;;+1/p-1
    Key: OESORJHGSXJTKX-UHFFFAOYSA-M
  • [C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[Mn].[Br-]
Properties
C5BrMnO5
Molar mass 274.892 g·mol−1
Appearanceorange solid
Hazards
GHS labelling:
GHS-pictogram-exclam.svg
Warning
H302, H312, H332
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Manganese pentacarbonyl bromide is an organomanganese compound with the formula BrMn(CO)5. It is a bright orange solid that is a precursor to other manganese complexes. The compound is prepared by treatment of dimanganese decacarbonyl with bromine: [1]

Mn2(CO)10 + Br2 → 2 BrMn(CO)5

The complex undergoes substitution by a variety of donor ligands (L), e.g. to give derivatives of the type BrMn(CO)3L2.

The complex adopts an octahedral coordination geometry. [2]

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3
COCHCOCH
3
) and metal ions, usually transition metals. The bidentate ligand acetylacetonate is often abbreviated acac. Typically both oxygen atoms bind to the metal to form a six-membered chelate ring. The simplest complexes have the formula M(acac)3 and M(acac)2. Mixed-ligand complexes, e.g. VO(acac)2, are also numerous. Variations of acetylacetonate have also been developed with myriad substituents in place of methyl (RCOCHCOR′). Many such complexes are soluble in organic solvents, in contrast to the related metal halides. Because of these properties, acac complexes are sometimes used as catalyst precursors and reagents. Applications include their use as NMR "shift reagents" and as catalysts for organic synthesis, and precursors to industrial hydroformylation catalysts. C
5
H
7
O
2
in some cases also binds to metals through the central carbon atom; this bonding mode is more common for the third-row transition metals such as platinum(II) and iridium(III).

Half sandwich compound Class of coordination compounds

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References

  1. King, R. B. (1965). Organometallic Syntheses. Volume 1 Transition-Metal Compounds. New York: Academic Press. ISBN   0444426078.
  2. J. G. Hernandez, I. S. Butler, T. Friščić (214). "Multi-step and multi-component organometallic synthesis in one pot using orthogonal mechanochemical reactions". Chemical Science. 5 (9): 3576. doi:10.1039/C4SC01252F.{{cite journal}}: CS1 maint: uses authors parameter (link)